Variant report

Variant	nsv873382
Chromosome Location	chr1:243034750-243119539
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:243088083-243088303	K562	blood:	n/a	n/a
2	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
3	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
4	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
5	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
6	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
7	CEBPB	chr1:243118303-243118616	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
8	CEBPB	chr1:243118255-243118634	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
9	CEBPB	chr1:243118280-243118602	IMR90	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
10	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
11	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
12	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
13	CEBPB	chr1:243118268-243118571	HepG2	liver:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
14	CEBPB	chr1:243088005-243088218	K562	blood:	n/a	n/a
15	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
16	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
17	CEBPB	chr1:243118344-243118540	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
18	CEBPB	chr1:243118300-243118585	A549	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
19	CEBPB	chr1:243118288-243118578	Hela-S3	cervix:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
20	CHD2	chr1:243087993-243088116	K562	blood:	n/a	n/a
21	CHD2	chr1:243080927-243080928	K562	blood:	n/a	n/a
22	CTCF	chr1:243100073-243100432	GM12878	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
23	CTCF	chr1:243099989-243100475	A549	lung:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
24	CTCF	chr1:243100149-243100294	SK-N-SH_RA	brain:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
25	CTCF	chr1:243100170-243100328	LNCaP	prostate:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
26	CTCF	chr1:243046760-243046910	GM12865	blood:	n/a	n/a
27	CTCF	chr1:243100128-243100360	HepG2	liver:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
28	CTCF	chr1:243100120-243100270	GM12864	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
29	CTCF	chr1:243045608-243045642	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:243100152-243100343	GM12878	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
31	CTCF	chr1:243074700-243074850	GM12875	blood:	n/a	n/a
32	CTCF	chr1:243100120-243100270	BE2_C	brain:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
33	CTCF	chr1:243100081-243100535	K562	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
34	CTCF	chr1:243063909-243063983	ProgFib	skin:	n/a	n/a
35	CTCF	chr1:243100100-243100250	HCT-116	colon:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
36	CTCF	chr1:243100100-243100250	GM12871	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
37	CTCF	chr1:243100124-243100385	GM19238	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
38	CTCF	chr1:243100100-243100250	HEK293	kidney:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
39	CTCF	chr1:243043213-243043217	K562	blood:	n/a	n/a
40	CTCF	chr1:243099979-243100540	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
41	CTCF	chr1:243095260-243095410	K562	blood:	n/a	chr1:243095371-243095381 chr1:243095368-243095386 chr1:243095363-243095384
42	CTCF	chr1:243100160-243100310	GM12867	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
43	CTCF	chr1:243100520-243100670	HEK293	kidney:	n/a	n/a
44	CTCF	chr1:243100200-243100350	GM12865	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
45	CTCF	chr1:243100121-243100385	A549	lung:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
46	CTCF	chr1:243100160-243100310	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
47	CTCF	chr1:243100152-243100357	Hela-S3	cervix:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
48	CTCF	chr1:243100162-243100338	GM13977	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
49	CTCF	chr1:243100540-243100690	HEK293	kidney:	n/a	n/a
50	CTCF	chr1:243049352-243049415	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243057080-243057130	T-47D	breast:	n/a
2	chr1:243057080-243057130	PFSK-1	brain:	n/a
3	chr1:243050875-243050925	HepG2	liver:	n/a
4	chr1:243053934-243053984	BJ	skin:	n/a
5	chr1:243057080-243057130	GM19239	blood:	n/a
6	chr1:243053425-243053475	GM19239	blood:	n/a
7	chr1:243050875-243050925	HIPEpiC	eye:	n/a
8	chr1:243053425-243053475	GM12878	blood:	n/a
9	chr1:243053934-243053984	HUVEC	blood vessel:	n/a
10	chr1:243053865-243053915	PrEC	prostate:	n/a
11	chr1:243054071-243054121	BE2_C	brain:	n/a
12	chr1:243053934-243053984	SK-N-SH	brain:	n/a
13	chr1:243054071-243054121	NH-A	brain:	n/a
14	chr1:243053865-243053915	MCF10A-Er-Src	breast:	n/a
15	chr1:243057080-243057130	HUVEC	blood vessel:	n/a
16	chr1:243053865-243053915	IMR90	lung:	fetal
17	chr1:243054071-243054121	HEEpiC	esophagus:	n/a
18	chr1:243053865-243053915	HIPEpiC	eye:	n/a
19	chr1:243053673-243053723	NT2-D1	testis:	n/a
20	chr1:243050875-243050925	GM19239	blood:	n/a
21	chr1:243053934-243053984	AG10803	skin:	n/a
22	chr1:243050875-243050925	NB4	blood:	n/a
23	chr1:243053425-243053475	ovcar-3	ovarian:	n/a
24	chr1:243054071-243054121	AG04450	lung:	fetal
25	chr1:243053425-243053475	GM12892	blood:	n/a
26	chr1:243053673-243053723	NHDF-neo	bronchial:	n/a
27	chr1:243053934-243053984	H1-hESC	embryonic stem cell:	embryo
28	chr1:243054071-243054121	CMK	blood:	n/a
29	chr1:243050875-243050925	HCPEpiC	choroid plexus:	n/a
30	chr1:243054071-243054121	GM12878	blood:	n/a
31	chr1:243057080-243057130	MCF-7	breast:	n/a
32	chr1:243053934-243053984	PrEC	prostate:	n/a
33	chr1:243057080-243057130	SK-N-MC	brain:	n/a
34	chr1:243053865-243053915	ECC-1	luminal epithelium:	n/a
35	chr1:243053673-243053723	HRPEpiC	eye:	n/a
36	chr1:243057080-243057130	GM12892	blood:	n/a
37	chr1:243053673-243053723	NB4	blood:	n/a
38	chr1:243053425-243053475	SAEC	small airway:	n/a
39	chr1:243054071-243054121	MCF-7	breast:	n/a
40	chr1:243054071-243054121	IMR90	lung:	fetal
41	chr1:243053934-243053984	CMK	blood:	n/a
42	chr1:243054071-243054121	NHDF-neo	bronchial:	n/a
43	chr1:243053934-243053984	MCF10A-Er-Src	breast:	n/a
44	chr1:243053865-243053915	GM12891	blood:	n/a
45	chr1:243053425-243053475	AoSMC	blood vessel:	n/a
46	chr1:243053865-243053915	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:243053425-243053475	GM06990	blood:	n/a
48	chr1:243057080-243057130	HMEC	breast:	n/a
49	chr1:243054071-243054121	HUVEC	blood vessel:	n/a
50	chr1:243053934-243053984	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
2	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
3	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
4	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-
2	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
3	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
4	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778
5	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-

Variant related genes	Relation type
ENSG00000270818	TF binding region
ENSG00000264972	TF binding region
ENSG00000270818	CpG island
ENSG00000264972	CpG island

Extended variants
information (count: 1520 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1520 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4233436	chr1:243034750-243034751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570200952	chr1:243034755-243034756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535939425	chr1:243034804-243034805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553587584	chr1:243034809-243034810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149326383	chr1:243034817-243034818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115060353	chr1:243034856-243034857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553994455	chr1:243034865-243034866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576767199	chr1:243034866-243034867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs193265235	chr1:243034873-243034874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114034130	chr1:243034878-243034879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184857383	chr1:243034928-243034929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563478145	chr1:243034941-243034942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187716800	chr1:243034981-243034982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561960006	chr1:243035048-243035049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527843951	chr1:243035100-243035101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576765485	chr1:243035167-243035168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144598537	chr1:243035256-243035257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564842675	chr1:243035264-243035265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191410713	chr1:243035273-243035274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374506630	chr1:243035377-243035378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369629998	chr1:243035396-243035397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372897407	chr1:243035400-243035401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565998205	chr1:243035415-243035416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550185173	chr1:243035427-243035428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58598293	chr1:243035430-243035431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35650197	chr1:243035459-243035460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35092228	chr1:243035473-243035474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138836518	chr1:243035479-243035480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183546207	chr1:243035480-243035481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549466165	chr1:243035580-243035581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188626039	chr1:243035596-243035597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181147143	chr1:243035604-243035605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553681437	chr1:243035609-243035610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570764181	chr1:243035625-243035626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539331624	chr1:243035628-243035629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555762454	chr1:243035638-243035639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs28361423	chr1:243035639-243035640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs12125155	chr1:243035660-243035661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554994706	chr1:243035702-243035703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112472676	chr1:243035712-243035713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572042307	chr1:243035735-243035736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146554982	chr1:243035738-243035739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372949426	chr1:243035782-243035783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189802623	chr1:243035804-243035805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146342117	chr1:243035833-243035834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181865372	chr1:243035838-243035839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544103211	chr1:243035842-243035843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563690603	chr1:243035862-243035863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529266576	chr1:243035876-243035877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs5028617	chr1:243035879-243035880	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:243033200-243042200	Enhancers	Fetal Heart	heart
2	chr1:243036400-243036800	Enhancers	Left Ventricle	heart
3	chr1:243036800-243039200	Weak transcription	Left Ventricle	heart
4	chr1:243038200-243039600	Enhancers	A549	lung
5	chr1:243039200-243042200	Enhancers	Left Ventricle	heart
6	chr1:243039400-243039600	Enhancers	Right Atrium	heart
7	chr1:243039600-243040000	Weak transcription	A549	lung
8	chr1:243039600-243040600	Weak transcription	Right Atrium	heart
9	chr1:243040000-243041400	Enhancers	A549	lung
10	chr1:243040200-243041000	Enhancers	Pancreas	Pancrea
11	chr1:243040200-243041400	Enhancers	K562	blood
12	chr1:243040600-243041000	Enhancers	Right Atrium	heart
13	chr1:243040600-243041000	Enhancers	Right Ventricle	heart
14	chr1:243040800-243041000	Bivalent Enhancer	Hela-S3	cervix
15	chr1:243040800-243042200	Enhancers	Liver	Liver
16	chr1:243041000-243043800	Weak transcription	Right Atrium	heart
17	chr1:243041000-243046600	Weak transcription	Pancreas	Pancrea
18	chr1:243041800-243042200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:243042000-243042600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr1:243042200-243044400	Weak transcription	Fetal Heart	heart
21	chr1:243044400-243045400	Enhancers	Fetal Heart	heart
22	chr1:243046600-243046800	Enhancers	Pancreas	Pancrea
23	chr1:243046800-243053600	Weak transcription	Pancreas	Pancrea
24	chr1:243047200-243049000	Weak transcription	A549	lung
25	chr1:243049000-243049200	Enhancers	A549	lung
26	chr1:243049200-243049800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:243049200-243049800	Enhancers	Liver	Liver
28	chr1:243049200-243049800	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr1:243049200-243049800	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr1:243049200-243049800	Flanking Active TSS	A549	lung
31	chr1:243049200-243049800	Enhancers	HepG2	liver
32	chr1:243049600-243049800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:243049800-243050600	Enhancers	A549	lung
34	chr1:243049800-243053600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr1:243049800-243053600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:243050600-243051800	Weak transcription	A549	lung
37	chr1:243053400-243053600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:243053600-243053800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:243053600-243054000	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr1:243053600-243054000	Active TSS	H1 Cell Line	embryonic stem cell
41	chr1:243053600-243054000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:243053600-243054000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:243053600-243054000	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:243053600-243054000	Active TSS	HUES6 Cell Line	embryonic stem cell
47	chr1:243053600-243054000	Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr1:243053600-243054000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr1:243053600-243054000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr1:243053600-243054000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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